[Technical Field]
[Cross-Reference to Related Applications]
[0001] This application claims priority to
Korean Patent Application No. 10-2019-0132824, filed on October 24, 2019,
Korean Patent Application No. 10-2019-0155393, filed on November 28, 2019,
Korean Patent Application No. 10-2019-0178383, filed on December 30, 2019, and
Korean Patent Application No. 10-2020-0131560, re-filed on October 13, 2020, based on the priority of the above three patents,
in the Korean Intellectual Property Office, the disclosures of each of which are incorporated
herein by reference.
[0002] The present invention relates to a polyester-based resin composition and a molded
article manufactured using the same. More particularly, the present invention relates
to a polyester-based resin composition having excellent fluidity, mechanical properties,
thermal stability, injection stability, and surface properties and a molded article
manufactured using the polyester-based resin composition. In particular, due to excellent
surface properties thereof, the polyester-based resin composition does not exhibit
iridescence caused by diffuse reflection. In addition, the polyester-based resin composition
has a low haze value. Accordingly, the polyester-based resin composition may be used
to manufacture a molded article such as an automotive headlamp bezel.
[Background Art]
[0003] In general, when automotive headlamp bezels are manufactured using polyester-based
resins. Automotive headlamps have different degrees of temperature rise when turned
on, depending on design, bulb type, or other factors. When an automotive headlamp
is heated to high temperature, an automotive headlamp bezel should be manufactured
using a resin having high heat resistance.
[0004] In addition, since automotive headlamp bezels are rather large and are manufactured
through high-speed injection molding, materials with low gas generation and excellent
surface properties are required.
[0005] When an automotive headlamp bezel is manufactured using a conventional polyester-based
resin, as a result of heat resistance evaluation after bezel deposition, fine cracks
are generated on the surface of the headlamp bezel due to difference in shrinkage
rates between an aluminum deposition layer and a resin layer, and iridescence caused
by diffuse reflection is exhibited. Thus, the automotive headlamp bezel has a poor
appearance. In addition, when a headlamp is turned on, materials that migrate from
the headlamp bezel are generated due to increase in temperature. These migrated materials
solidify on the inner surface of a headlamp lens, lowering the light transmittance
of the headlamp.
[0006] Conventionally, in consideration of injection workability, resins having high fluidity
have been used when manufacturing headlamp bezels. However, there is a problem in
that the surface quality of an injection product deteriorates due to generation of
gas derived from low molecular weight oligomers contained in a resin having high fluidity
during injection. In addition, there is another problem in that pressure deviation
occurs during injection.
[0007] Therefore, a material having excellent injection moldability, injection stability,
and mechanical properties and having improved thermal stability and appearance properties
needs to be developed.
[Disclosure]
[Technical Problem]
[0008] Therefore, the present invention has been made to solve the above problems, and it
is one object of the present invention to provide a polyester-based resin composition
having excellent fluidity, mechanical properties, thermal stability, injection stability,
and surface properties and a molded article manufactured using the same. In particular,
due to excellent surface properties thereof, the polyester-based resin composition
does not exhibit iridescence caused by diffuse reflection. In addition, the polyester-based
resin composition has a low haze value. Accordingly, the polyester-based resin composition
may be used to manufacture a molded article such as an automotive headlamp bezel.
[0009] It is another object of the present invention to provide a polyester-based resin
composition used for making an automotive headlamp bezel having a low haze value and
excellent mechanical properties and an automotive headlamp bezel manufactured using
the same.
[0010] However, problems to be solved by the present invention are not limited to the above-described
problems, and other problems that are not mentioned will be clearly understood by
those skilled in the art from the following description.
[0011] The above and other objects can be accomplished by the present disclosure described
below.
[Technical Solution]
[0012] In accordance with one aspect of the present invention, provided is a polyester-based
resin composition including 93 to 99.5 % by weight of a polybutylene terephthalate
resin; 0.1 to 3 % by weight of a polar group-containing lubricant; and 0.1 to 2 %
by weight of an antioxidant.
[0013] Preferably, the polybutylene terephthalate resin may have an intrinsic viscosity
of 0.90 to 1.15 dl/g.
[0014] In the present invention, intrinsic viscosity may be measured using a Canon viscometer
after completely dissolving 2 g of a polybutylene terephthalate resin in 25 ml of
2-chlorophenol.
[0015] Preferably, the polybutylene terephthalate resin may include a first polybutylene
terephthalate resin having a relative viscosity of 0.95 to 1 as measured according
to ASTM D1243 and a second polybutylene terephthalate resin having a relative viscosity
of 0.75 to 0.8 as measured according to ASTM D1243.
[0016] Preferably, the polar group-containing lubricant may be a lubricant containing at
least one polar group of a hydroxyl group, a carbonyl group, and an amino group.
[0017] Preferably, the polar group-containing lubricant may have a dropping point of 115
to 128 °C or a crystallization temperature (Tm) of 102 to 122 °C.
[0018] In the present invention, dropping point indicates the minimum temperature at which
a lubricant is transformed to a liquid when raising temperature according to ASTM
D566, KS M 2033. More specifically, a sample is placed in a specified cup having a
diameter of 100 mm and the sample is heated according to the specified conditions.
Then, a temperature at which grease drops is measured. In this case, the temperature
represents a dropping point.
[0019] In the present invention, crystallization temperature refers to a temperature at
which crystallization occurs. In this case, crystallization means that the structure
of a substance is converted from an irregular arrangement into a regular arrangement
by attraction between molecules/atoms, and crystallization temperature may be measured
using a differential scanning calorimeter (DSC). As a specific example of crystallization
temperature measurement, a measurement container is filled with approximately 0.5
mg to 10 mg of a sample, and the flow rate of nitrogen gas is set to 20 ml/min. To
make the thermal history of the sample the same, temperature is raised from 0 °C to
150 °C at a rate of 20 °C/min, and then maintained for 2 minutes in that state. Then,
heat flow is measured using a DSC while cooling from 150 °C to -100 °C at a rate of
10 °C/min. At this time, the peak of the cooling curve of heat flow, i.e., the temperature
of an exothermic peak during cooling, is crystallization temperature. At this case,
"peak" means a vertex of the cooling curve or a heating curve to be described later.
For example, based on a point where the slope of a tangent line is 0, inflection points
where the sign of the slope value of the tangent line changes are excluded.
[0020] Preferably, the polar group-containing lubricant may be a lubricant containing two
or more polar groups at the terminal thereof, more preferably a lubricant containing
two to five polar groups at the terminal thereof.
[0021] Preferably, the antioxidant may be a phenolic antioxidant.
[0022] Preferably, the polyester-based resin composition may further include a hydrolysis
stabilizer.
[0023] Preferably, the hydrolysis stabilizer may be included in an amount of 0.01 to 2 %
by weight.
[0024] Preferably, the hydrolysis stabilizer may be an aromatic group-containing polycarbodiimide-based
compound.
[0025] Preferably, the polyester-based resin composition may further include a styrene-acrylonitrile
copolymer.
[0026] Preferably, the styrene-acrylonitrile copolymer may be included in an amount of 0.5
to 6 % by weight.
[0027] Preferably, the styrene-acrylonitrile copolymer may be a copolymer including 71 to
75 % by weight of styrene and 25 to 29 % by weight of acrylonitrile.
[0028] Preferably, the polyester-based resin composition may have a haze value of 10 or
less.
[0029] In accordance with another aspect of the present invention, provided is a molded
article manufactured by extruding or injecting the polyester-based resin composition.
[0030] In this case, extruding may be performed by adding the components of the polyester-based
resin composition into a super mixer, homogenizing the components, melting and kneading
the mixture using a twin-screw extruder at 240 to 270 °C, and performing extrusion
to prepare a pellet.
[0031] Preferably, the molded article may be an automotive headlamp bezel.
[0032] Preferably, the molded article may have a haze value of 10 or less, more preferably
5 or less, at 130 to 160 °C.
[0033] In accordance with still another aspect of the present invention, provided is a polyester-based
resin composition including a polybutylene terephthalate resin; a polar group-containing
lubricant; an antioxidant; and a hydrolysis stabilizer.
[0034] In accordance with still another aspect of the present invention, provided is a polyester-based
resin composition including a polybutylene terephthalate having an intrinsic viscosity
of 0.90 to 1.15 dl/g; an ester group-containing lubricant; an antioxidant; and a hydrolysis
stabilizer.
[0035] In accordance with still another aspect of the present invention, provided is a composition
for automotive headlamp bezels, the composition including a polybutylene terephthalate
resin and a styrene-acrylonitrile copolymer, wherein the styrene-acrylonitrile copolymer
includes 25 to 29 % by weight of acrylonitrile.
[0036] In accordance with yet another aspect of the present invention, provided is a method
of manufacturing an automotive headlamp bezel, the method including an injection step
of injecting the polyester-based resin composition to manufacture a molded article;
a painting step of painting the manufactured molded article; and a deposition step
of depositing aluminum on the painted molded article.
[0037] Preferably, the injecting step may be performed under conditions of an injection
temperature of 240 to 270 °C and a mold temperature of 100 to 120 °C.
[Advantageous effects]
[0038] According to the present invention, a polyester-based resin composition having excellent
fluidity, mechanical properties, thermal stability, injection stability, and surface
properties and a molded article manufactured using the same can be provided. In particular,
due to excellent surface properties thereof, the polyester-based resin composition
does not exhibit iridescence caused by diffuse reflection. In addition, the polyester-based
resin composition has a low haze value. Accordingly, the polyester-based resin composition
can be used to manufacture a molded article such as an automotive headlamp bezel.
[0039] The effects of the present invention are not limited to the above-described effects,
and effects that are not mentioned will be clearly understood by those skilled in
the art through the specification and the accompanying drawings.
[Description of Drawings]
[0040]
FIG. 1 includes drawings for explaining a method of evaluating the amount of gas generated
when molding a polyester-based resin composition according to one embodiment of the
present invention.
FIG. 2 shows the results of a whitening test performed on the specimens of Examples
1 to 3 and Example 5 and Comparative Examples 2 to 5 according to the present invention.
FIG. 3 shows a Discovery Hybrid Rheometer (DHR) for measuring the viscosity of a polyester-based
resin composition according to one embodiment of the present invention.
FIG. 4 is an image of a specimen when the spiral flow length of a polyester-based
resin composition according to one embodiment of the present invention is measured.
FIG. 5 includes an image and a drawing for explaining a method of evaluating the haze
of a composition according to one embodiment of the present invention.
FIG. 6 includes images of a specimen in which iridescence occurs.
[Best mode]
[0041] In the present invention, it is to be understood that, unless otherwise stated, when
a part "comprises" any element, the part may include other elements without excluding
other elements.
[0042] In the present invention, when a member is located "on" the other member, this includes
not only the case where the member is in contact with the other member but also the
case where another member is present between the two members.
[0043] Throughout this specification, a unit "part by weight" may mean a weight ratio between
components.
[0044] Hereinafter, the present invention will be described in detail.
[0045] According to one embodiment of the present invention, a polyester-based resin composition
including a polybutylene terephthalate resin; a polar group-containing lubricant;
an antioxidant; and a hydrolysis stabilizer is provided. In this case, the polyester-based
resin composition may have excellent mechanical properties and thermal stability.
[0046] According to another embodiment of the present invention, a polyester-based resin
composition including a polybutylene terephthalate having an intrinsic viscosity of
0.90 dl/g to 1.15 dl/g; an ester group-containing lubricant; an antioxidant; and a
hydrolysis stabilizer is provided. In this case, the polyester-based resin composition
may have excellent mechanical properties and injection stability.
[0047] According to another embodiment of the present invention, a composition for automotive
headlamp bezels including a polybutylene terephthalate resin and a styrene-acrylonitrile
copolymer, wherein the styrene-acrylonitrile copolymer includes 25 to 29 % by weight
of acrylonitrile, is provided. In this case, the composition for automotive headlamp
bezels may have excellent fluidity, mechanical properties, and injection stability,
may have a low haze value, and may not exhibit iridescence. Thus, the composition
for automotive headlamp bezels may be suitably used in manufacture of an automotive
headlamp bezel.
[0048] According to another embodiment of the present invention, a polyester-based resin
composition including 93 to 99.5 % by weight of a polybutylene terephthalate resin;
0.1 to 3 % by weight of a polar group-containing lubricant; and 0.1 to 2 % by weight
of an antioxidant is provided. In this case, the polyester-based resin composition
may have excellent mechanical properties, thermal stability, surface properties, and
injection stability, may have a low haze value, and may not exhibit iridescence. Thus,
the polyester-based resin composition may be suitably used in manufacture of an automotive
headlamp bezel.
[0049] According to one embodiment of the present invention, the polybutylene terephthalate
may have an intrinsic viscosity of 0.90 dl/g to 1.15 dl/g. Specifically, the polybutylene
terephthalate may have an intrinsic viscosity of 0.91 dl/g to 1.14 dl/g, 0.91 dl/g
to 1.12 dl/g, 0.93 dl/g to 1.10 dl/g, 0.95 dl/g to 1.08 dl/g, 0.97 dl/g to 1.05 dl/g,
or 1.00 dl/g to 1.03 dl/g.
[0050] More specifically, the polybutylene terephthalate may have an intrinsic viscosity
of 0.90 dl/g to 0.95 dl/g, 0.96 dl/g to 0.99 dl/g, 1.01 dl/g to 1.06 dl/g, 1.08 dl/g
to 1.12 dl/g, or 1.13 dl/g to 1.15 dl/g.
[0051] A polyester-based resin composition including a polybutylene terephthalate having
an intrinsic viscosity within the above-described range may have excellent mechanical
properties and injection stability. In addition, by using a polybutylene terephthalate
having an intrinsic viscosity within the above range, a polyester-based resin composition
having good fluidity and excellent surface quality may be provided.
[0052] According to one embodiment of the present invention, based on 100 parts by weight
of the polyester-based resin composition, the polybutylene terephthalate resin may
be included in an amount of 95 parts by weight to 99.5 parts by weight. Specifically,
based on 100 parts by weight of the polyester-based resin composition, the polybutylene
terephthalate resin may be included in an amount of 97 parts by weight to 99.5 parts
by weight, 95 parts by weight to 98 parts by weight, or 99 parts by weight to 99.5
parts by weight. By adjusting the content of the polybutylene terephthalate resin
included in the polyester-based resin composition within the above-described range,
a polyester-based composition having excellent mechanical properties may be provided.
In addition, a molded article manufactured using the polyester-based resin composition
may have excellent surface properties.
[0053] According to one embodiment of the present invention, the polybutylene terephthalate
resin may include two or more polybutylene terephthalate resins each having different
viscosity. Specifically, the polybutylene terephthalate resin may include a first
polybutylene terephthalate resin having a relative viscosity of 0.95 to 1 as measured
according to ASTM D1243 and a second polybutylene terephthalate resin having a relative
viscosity of 0.75 to 0.8 as measured according to ASTM D1243. When the first and second
polybutylene terephthalate resins are included within the above-described ranges,
a polyester-based resin composition having excellent mechanical properties may be
provided.
[0054] Relative viscosity may be measured according to ASTM D1243. Specifically, a polybutylene
terephthalate resin may be dissolved in any one solvent of a mixed solution of phenol
and 1,2-dichlorobenzene; o-chlorophenol; a mixed solution of phenol and 1,1,2,2-tetrachloroethane;
and m-cresol, and then the relative viscosity of the dissolved resin may be measured.
[0055] According to one embodiment of the present invention, the first polybutylene terephthalate
resin and the second polybutylene terephthalate resin may be included in a weight
ratio of 2:1 to 1:2. When the first and second polybutylene terephthalate resins are
included in a weight ratio within this range, a molded article manufactured using
the composition for automotive headlamp bezels may have excellent surface properties.
[0056] According to one embodiment of the present invention, based on 100 parts by weight
of the first polybutylene terephthalate resin, the second polybutylene terephthalate
resin may be included in an amount of 60 to 80 parts by weight or 69 to 77 parts by
weight.
[0057] According to one embodiment of the present invention, based on 100 parts by weight
of the polyester-based resin composition, the polar group-containing lubricant may
be included in an amount of 0.1 parts by weight to 3 parts by weight. Specifically,
based on 100 parts by weight of the polyester-based resin composition, the polar group-containing
lubricant may be included in an amount of 0.2 parts by weight to 2.5 parts by weight,
0.4 parts by weight to 2 parts by weight, 0.2 parts by weight to 1 part by weight,
1.5 parts by weight to 2.2 parts by weight, or 2 parts by weight to 3 parts by weight.
By adjusting the content of the lubricant included in the polyester-based resin composition
within the above-described range, the polyester-based resin composition may have excellent
thermal stability, and due to the low volatility thereof, gas generation may be prevented
during molding. In addition, the polyester-based resin composition may have excellent
processability and moldability.
[0058] According to another embodiment of the present invention, based on 100 parts by weight
of the polyester-based resin composition, the ester group-containing lubricant may
be included in an amount of greater than 0 parts by weight and less than or equal
to 1 part by weight, preferably 0.1 parts by weight to 1 part by weight. Specifically,
based on 100 parts by weight of the polyester-based resin composition, the ester group-containing
lubricant may be included in an amount of 0.2 parts by weight to 0.8 parts by weight,
or 0.3 parts by weight to 0.6 parts by weight. More specifically, based on 100 parts
by weight of the polyester-based resin composition, the ester group-containing lubricant
may be included in an amount of 0.1 parts by weight to 0.3 parts by weight, 0.2 parts
by weight to 0.5 parts by weight, or 0.6 parts by weight to 1 part by weight. By adjusting
the content of the lubricant included in the polyester-based resin composition within
the above-described range, the polyester-based resin composition may have excellent
injection stability, and due to the low volatility thereof, gas generation may be
prevented during molding. In addition, the polyester-based resin composition may have
excellent processability and moldability.
[0059] According to one embodiment of the present invention, the polar group-containing
lubricant may include a polyolefin containing at least one polar group of a hydroxyl
group, a carbonyl group, and an amino group. Specifically, the carbonyl group may
be a carboxyl group or an ester group. Specifically, the polar group-containing lubricant
preferably includes a hydroxyl group. By using the lubricant containing the above-described
polar group, the thermal stability of the polyester-based resin composition may be
efficiently improved without deterioration in the physical properties thereof.
[0060] For example, the lubricant may be prepared by polymerizing olefins having 1 to 5
carbon atoms. Specifically, the lubricant may be a polymer consisting of monomers
including olefins containing at least the polar group and 1 to 5 carbon atoms. The
lubricant including a polymer of olefins containing a polar group and 1 to 5 carbon
atoms has excellent thermal stability and low volatility, and thus a polyester-based
resin composition including the lubricant may have excellent thermal stability and
moldability.
[0061] According to one embodiment of the present invention, the lubricant may include an
ester group. By using an ester group-containing lubricant, the polyester-based resin
composition may have good fluidity, thereby improving the processability and moldability
thereof. In addition, since the lubricant containing an ester group has low volatility,
gas generation may be prevented during injection molding of a polyester-based resin
composition including the lubricant.
[0062] According to one embodiment of the present invention, the lubricant may include pentaerythritol-based
lubricants. For example, the lubricant may include pentaerythritol monoester compounds
such as pentaerythritol monostearate, pentaerythritol distearate, and pentaerythritol
tetrastearate or pentaerythritol diester compounds.
[0063] According to one embodiment of the present invention, the weight ratio of the lubricant
to the polybutylene terephthalate resin may be 1:40 to 1:250. Specifically, the weight
ratio of the lubricant to the polybutylene terephthalate resin may be 1:45 to 1:250,
1:40 to 1:50, or 1:200 to 1:250. By adjusting the weight ratio of the lubricant to
the polybutylene terephthalate resin within the above-described range, a polyester-based
resin composition having excellent mechanical properties and thermal stability may
be provided. In addition, the polyester-based resin composition may have excellent
processability and moldability.
[0064] According to another embodiment of the present invention, the weight ratio of the
lubricant to the polybutylene terephthalate may be 1:250 to 1:350. Specifically, the
weight ratio of the lubricant to the polybutylene terephthalate may be 1:270 to 1:340,
1:285 to 1:330, 1:290 to 1:320, or 1:300 to 1:310. More specifically, the weight ratio
of the lubricant to the polybutylene terephthalate may be 1:250 to 1:280, 1:290 to
1:330, 1:300 to 1:330, 1:315 to 1:330, or 1:320 to 1:350.
[0065] By adjusting the weight ratio of the lubricant to the polybutylene terephthalate
within the above-described range, a polyester-based resin composition having excellent
mechanical properties and injection stability may be provided. In addition, the polyester-based
resin composition may have excellent processability and surface quality.
[0066] According to one embodiment of the present invention, based on 100 parts by weight
of the polyester-based resin composition, the antioxidant may be included in an amount
of greater than 0 parts by weight and less than or equal to 1 part by weight, preferably
0.1 parts by weight to 1 part by weight. Specifically, based on 100 parts by weight
of the polyester-based resin composition, the antioxidant may be included in an amount
of 0.2 parts by weight to 0.7 parts by weight, 0.2 parts by weight to 0.5 parts by
weight, or 0.1 parts by weight to 0.3 parts by weight. When the antioxidant is included
in the polyester-based resin composition within this content range, the polyester-based
resin composition may be prevented from discoloring. In addition, by adjusting the
content of the antioxidant within the above-described range, cleavage or crosslinking
of the molecular chains of polymers included in the polyester-based resin composition
due to oxidation may be suppressed, thereby preventing degradation of physical properties.
[0067] According to another embodiment of the present invention, based on 100 parts by weight
of the polyester-based resin composition, the antioxidant may be included in an amount
of 0.1 to 0.5 parts by weight.
[0068] Specifically, based on 100 parts by weight of the polyester-based resin composition,
the antioxidant may be included in an amount of 0.2 to 0.7 parts by weight, 0.2 to
0.5 parts by weight, or 0.1 to 0.3 parts by weight. When the antioxidant is included
in the polyester-based resin composition within this content range, the polyester-based
resin composition may be prevented from discoloring. In addition, by adjusting the
content of the antioxidant within the above-described range, cleavage or crosslinking
of the molecular chains of polymers included in the polyester-based resin composition
due to oxidation may be suppressed, thereby preventing degradation of physical properties.
[0069] According to one embodiment of the present invention, the antioxidant may include
a phenolic antioxidant. By using the phenolic antioxidant, polymers included in the
polyester-based composition may be further stabilized. Specifically, the phenolic
antioxidant may serve to protect the polyester-based composition by removing the radicals
of polymers included in the polyester-based resin composition during molding of the
polyester-based resin composition.
[0070] The phenolic antioxidant preferably includes one or more selected from tetrakis[ethylene-3-(3,5-di-t-butyl-hydroxy
phenyl)propionate] (IR-1010), octadecyl 3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate
(IR-1076), pentaerythritol tetrakis[3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate],
and 1,3,5-trimethyl-2,4,6-tris(3,5-di-t-butyl-4-hydroxybenzyl)benzene. More preferably,
the phenolic antioxidant is octadecyl 3-(3,5-di-t-butyl-4-hydroxyphenyl)propionate
(IR-1076), still more preferably Hindered Phenolic Antioxidant 1010.
[0071] According to one embodiment of the present invention, based on 100 parts by weight
of the polyester-based resin composition, the hydrolysis stabilizer may be included
in an amount of 0.01 parts by weight to 0.5 parts by weight. Specifically, based on
100 parts by weight of the polyester-based resin composition, the hydrolysis stabilizer
may be included in an amount of 0.01 parts by weight to 0.2 parts by weight, 0.02
parts by weight to 0.15 parts by weight, 0.04 parts by weight to 0.1 parts by weight,
0.01 parts by weight to 0.07 parts by weight, or 0.05 parts by weight to 0.12 parts
by weight. By adjusting the content of the hydrolysis stabilizer included in the polyester-based
resin composition within the above-described range, the hydrolysis resistance of the
polyester-based resin composition may be effectively improved. Thereby, volatile gas
components generated from the polyester-based resin composition may be reduced, and
deterioration in fluidity during injecting may be prevented.
[0072] According to another embodiment of the present invention, based on 100 parts by weight
of the polyester-based resin composition, the hydrolysis stabilizer may be included
in an amount of greater than 0 parts by weight and less than or equal to 1 part by
weight, preferably 0.1 parts by weight to 1 part by weight. Specifically, based on
100 parts by weight of the polyester-based resin composition, the hydrolysis stabilizer
may be included in an amount of 0.2 parts by weight to 0.8 parts by weight, 0.3 parts
by weight to 0.7 parts by weight, or 0.4 parts by weight to 0.6 parts by weight. By
adjusting the content of the hydrolysis stabilizer included in the polyester-based
resin composition within the above-described range, the hydrolysis resistance of the
polyester-based resin composition may be effectively improved. Thereby, volatile gas
components generated from the polyester-based resin composition may be reduced, and
deterioration in fluidity during injecting may be prevented.
[0073] According to one embodiment of the present invention, the hydrolysis stabilizer may
include aromatic group-containing polycarbodiimide-based compounds. Specifically,
the hydrolysis stabilizer may include phenyl group-containing polycarbodiimides. When
an aromatic group-containing polycarbodiimide-based compound is used as the hydrolysis
stabilizer, gas generation during molding of the polyester-based resin composition
may be effectively prevented.
[0074] For example, the aromatic group-containing polycarbodiimide-based compound may be
a homopolymer or copolymer consisting of one or more aromatic carbodiimide compounds.
As a specific example, the aromatic group-containing polycarbodiimide compound may
include a compound represented by Chemical Formula 1 below. In this case, the polyester-based
resin composition may have excellent mechanical properties and hydrolysis resistance,
and the polyester-based resin composition may be suitably used for manufacture of
automotive headlamp bezels.

[0075] In Chemical Formula 1, n is an integer of 1 to 20.
[0076] For example, the aromatic group-containing polycarbodiimide-based compound represented
by Chemical Formula 1 may be prepared according to Reaction Formula 1 below.
[0077]

[0078] In Reaction Formula 1, DIPPI and TRIDI are carbodiimide compounds as precursors,
+T means heating to a predetermined reaction temperature, and -CO
2 means that CO
2 is removed from the precursors during reaction.
[0079] For example, the aromatic carbodiimide compound may include one or more selected
from the group consisting of N,N'-di-o-tolylcarbodiimide, N,N'-di-2,6-diketylphenylcarbodiimide,
N-tolyl-N'-cyclohexylcarbodiimide, N,N'-di-2,6-diisopropylphenylcarbodiimide, N,N'-di-2,6-di-tertiary-butylphenylcarbodiimide,
N-tolyl-N'-phenylcarbodiimide, N,N'-di-p-nitrophenylcarbodiimide, N,N'-di-p-aminophenylcarbodiimide,
N,N'-di-p-hydroxyphenylcarbodiimide, N,N'-di-p-tolylcarbodiimide, p-propylene-bis-di-o-tolylcarbodiimide,
p-propylene-bisdicyclohexylcarbodiimide, ethylene-bisdiphenylcarbodiimide, benzene-2,4-diisocyanato-1,3,5-tris(1-methylethyl),
and 2,4-diisocyanato-1,3,5-tris(1-methylethyl).
[0080] As another example, the aromatic group-containing polycarbodiimide-based compound
may include one or more selected from the group consisting of a benzene-2,4-diisocyanato-1,3,5-tris(1-methylethyl)
homopolymer; and a copolymer of 2,4-diisocyanato-1,3,5-tris(1-methylethyl) and 2,6-diisopropyl
diisocyanate.
[0081] For example, the aromatic group-containing polycarbodiimide-based compound may have
a weight average molecular weight of 500 to 4,000 g/mol or 1,000 to 3,500 g/mol. Within
this range, mechanical properties may be excellent.
[0082] In this description, unless otherwise defined herein, weight average molecular weight
may be measured using gel permeation chromatography (GPC, Waters Breeze). As a specific
example, weight average molecular weight may be measured using tetrahydrofuran (THF)
as an eluate through gel permeation chromatography (GPC, Waters Breeze). In this case,
weight average molecular weight is obtained as a relative value to a standard polystyrene
(PS) specimen.
[0083] According to one embodiment of the present invention, based on 100 parts by weight
of the polybutylene terephthalate resin, the total weight of the lubricant, the antioxidant,
and the hydrolysis stabilizer as additives may be greater than 0 parts by weight and
less than or equal to 3 parts by weight, or 0.1 parts by weight to 3 parts by weight.
[0084] According to one embodiment of the present invention, the styrene-acrylonitrile copolymer
may include 25 to 29 % by weight, 26 to 29 % by weight, or 28 to 29 % by weight of
acrylonitrile. When the styrene-acrylonitrile copolymer including acrylonitrile within
this content range is used, the composition for automotive headlamp bezels may have
excellent mold shrinkage, and thus the release properties thereof may be improved.
This effect may be clearly confirmed especially when a molded article is relatively
large.
[0085] According to one embodiment of the present invention, based on 100 parts by weight
of the polybutylene terephthalate resin, the styrene-acrylonitrile copolymer may be
included in an amount of 1 to 15 parts by weight, 3 to 10 parts by weight, or 5 to
10 parts by weight. Within this range, the composition for automotive headlamp bezels
may have excellent injection moldability.
[0086] According to one embodiment of the present invention, based on the total weight of
the composition for automotive headlamp bezels, the styrene-acrylonitrile copolymer
may be included in an amount of 1 to 10 % by weight or 1 to 5 % by weight.
[0087] The composition for automotive headlamp bezels according to one embodiment of the
present invention may include a polyethylene terephthalate resin. When the polyethylene
terephthalate resin is added, appearance may be further improved. However, due to
the low polymer crystallization rate of the polyethylene terephthalate resin, moldability
may deteriorate. Thus, based on the total weight of the composition for automotive
headlamp bezels, the polyethylene terephthalate resin is preferably included in an
amount of 1 to 10 % by weight.
[0088] According to one embodiment of the present invention, the composition for automotive
headlamp bezels may have a haze value of 10 or less, 8 or less, 7 or less, or 6 or
less. Within this range, from a lamp light source, projection ability in the front
direction may be excellent.
[0089] According to one embodiment of the present invention, a bezel for lamps including
a molded article manufactured using a polyester-based resin composition is provided.
The bezel for lamps may have excellent thermal stability.
[0090] A polyester-based resin composition used to form a bezel for lamps according to one
embodiment of the present invention may be the same as the polyester-based resin composition
according to one embodiment described above. That is, according to one embodiment
of the present invention, a bezel for lamps including a molded article manufactured
using a polyester-based resin composition including a polybutylene terephthalate resin;
a polar group-containing lubricant; an antioxidant; and a hydrolysis stabilizer is
provided.
[0091] In addition, a polyester-based resin composition used to form a bezel for lamps according
to another embodiment of the present invention may be the same as the polyester-based
resin composition according to one embodiment described above. That is, according
to one embodiment of the present invention, a bezel for lamps including a molded article
manufactured using a polyester-based resin composition including a polybutylene terephthalate
having an intrinsic viscosity of 0.90 dl/g to 1.15 dl/g; an ester group-containing
lubricant; an antioxidant; and a hydrolysis stabilizer is provided.
[0092] According to one embodiment of the present invention, the bezel for lamps may include
an injection-molded product or an extrusion-molded product manufactured using the
polyester-based resin composition. That is, the bezel for lamps may be formed by injection
molding or extrusion molding the polyester-based resin composition. By using a method
commonly used in the art without limitation, the polyester-based resin composition
may be injection-molded or extrusion-molded.
[0093] According to one embodiment of the present invention, the bezel for lamps may not
exhibit whitening at a temperature of 130 °C to 160 °C. As described above, in the
case of the bezel for lamps including a molded article manufactured using the polyester-based
resin composition having excellent thermal stability, occurrence of whitening due
to surface migration at high temperature may be suppressed. In addition, the bezel
for lamps may have excellent mechanical properties and surface quality. In addition,
the bezel for lamps may have a low haze value and excellent surface properties such
as paintability and evaporation properties.
[0094] According to one embodiment of the present invention, the bezel for lamps may be
an automotive headlamp bezel. As described above, since the bezel for lamps has excellent
thermal stability, surface properties, and mechanical properties, excellent surface
properties such as paintability and evaporation properties, and a low haze value,
the bezel for lamps may be used as an automotive headlamp bezel.
[0095] The automotive headlamp bezel according to another embodiment of the present invention
may be manufactured by depositing metal such as aluminum on the surface of a molded
article manufactured using a composition for automotive headlamp bezels. As a specific
example, the automotive headlamp bezel may be manufactured through injection, painting,
and aluminum deposition processes.
[0096] Hereinafter, the present invention will be described in more detail with reference
to the following preferred examples. However, these examples are provided for illustrative
purposes only and should not be construed as limiting the scope and spirit of the
present invention. In addition, it will be apparent to those skilled in the art that
various changes and modifications may be made without departing from the spirit and
scope of the present invention, and such changes and modifications are also within
the scope of the appended claims.
[Examples]
<Preparation of polyester-based resin composition>
Example 1
[0097] A polybutylene terephthalate resin, carbonyl group-containing polyethylene wax having
a dropping point of approximately 123 °C or less and a crystallization temperature
(Tm) of approximately 121 °C as a polar group-containing lubricant, a phenolic antioxidant
as an antioxidant, and a phenyl group-containing polycarbodiimide as a hydrolysis
stabilizer were mixed to prepare a polyester-based resin composition.
[0098] In this case, based on 100 parts by weight of the polyester-based resin composition,
the content of the polybutylene terephthalate resin was 99.2 parts by weight, the
content of the polar group-containing lubricant was 0.1 parts by weight, the content
of the antioxidant was 0.2 parts by weight, and the content of the hydrolysis stabilizer
was 0.5 parts by weight.
Examples 2 to 5
[0099] A polyester-based resin composition was prepared in the same manner as in Example
1, except that the contents of each of the polybutylene terephthalate resin, the polar
group-containing lubricant, the antioxidant, and the hydrolysis stabilizer were adjusted
as shown in Table 1 below.
Additional Example 1
[0100] A polyester-based resin composition was prepared in the same manner as in Example
1, except that a montanic acid ester having a dropping point of approximately 74 °C
or less and a crystallization temperature (Tm) of approximately 66 °C was used instead
of the polar group-containing lubricant used in Example 1 and the contents of each
of the polybutylene terephthalate resin, the montanic acid ester, the antioxidant,
and the hydrolysis stabilizer were adjusted as shown in Table 1 below.
Additional Example 2
[0101] A polyester-based resin composition was prepared in the same manner as in Example
1, except that pentaerythritol tetrastearate having a dropping point of approximately
60 °C to 63 °C and a crystallization temperature (Tm) of approximately 59 °C was used
instead of the polar group-containing lubricant used in Example 1 and the contents
of each of the polybutylene terephthalate resin, pentaerythritol tetrastearate, the
antioxidant, and the hydrolysis stabilizer were adjusted as shown in Table 1 below.
Additional Example 3
[0102] A polyester-based resin composition was prepared in the same manner as in Additionl
Example 1, except that the contents of each of the polybutylene terephthalate resin,
a montanic acid ester having a dropping point of approximately 74 °C or less and a
crystallization temperature (Tm) of approximately 66 °C, the antioxidant, and the
hydrolysis stabilizer were adjusted as shown in Table 1 below.
Additional Example 4
[0103] A polyester-based resin composition was prepared in the same manner as in Example
1, except that a partially saponified montanic acid ester having a dropping point
of approximately 105 °C or less and a crystallization temperature (Tm) of approximately
81 °C was used instead of the polar group-containing lubricant used in Example 1 and
the contents of each of the polybutylene terephthalate resin, the partially saponified
montanic acid ester, the antioxidant, and the hydrolysis stabilizer were adjusted
as shown in Table 1 below.
Comparative Example 1
[0104] A polyester-based resin composition was prepared in the same manner as in Example
1, except that polar group-free polyethylene wax having a dropping point of approximately
135 °C or less and a crystallization temperature (Tm) of approximately 124 °C was
used instead of the polar group-containing lubricant used in Example 1 and the contents
of each of the polybutylene terephthalate resin, the polar group-free polyethylene
wax, the antioxidant, and the hydrolysis stabilizer were adjusted as shown in Table
1 below.
[Table 1]
| Parts by weight |
Examples |
Additional Examples |
Comparative Example |
| 1 |
2 |
3 |
4 |
5 |
1 |
2 |
3 |
4 |
1 |
| A |
99.2 |
99.1 |
98.9 |
98.5 |
98.3 |
99.1 |
99.1 |
99.1 |
99.1 |
99.1 |
| B1 |
|
|
|
|
|
|
0.2 |
|
|
|
| B2 |
|
|
|
|
|
0.2 |
|
0.4 |
|
|
| B3 |
|
|
|
|
|
|
|
|
0.2 |
|
| B4 |
0.1 |
0.2 |
0.8 |
1.0 |
2.0 |
|
|
|
|
|
| B5 |
|
|
|
|
|
|
|
|
|
0.2 |
| C |
0.2 |
0.2 |
0.2 |
0.2 |
0.2 |
0.2 |
0.2 |
0.2 |
0.2 |
0.2 |
| D |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
[0105] In Table 1, "A" represents the polybutylene terephthalate resin, "B1" represents
pentaerythritol tetrastearate, "B2" represents the montanic acid ester, "B3" represents
the partially saponified montanic acid ester, "B4" represents the carbonyl group-containing
polyethylene wax, "B5" represents the polar group-free polyethylene wax, "C" represents
the phenolic antioxidant, and "D" represents the phenyl group-containing polycarbodiimide.
In addition, in Table 1, the content of each component is given in parts by weight
based on 100 parts by weight of the polyester-based resin composition.
[Preparation of specimens for measuring physical properties]
[0106] Each of polyester-based resin compositions according to Examples 1 to 5, Additional
Examples 1 to 4, and Comparative Example 1 formulated according to the components
and contents specified in Table 1 was added to a super mixer and homogenizied, was
melted and kneaded using a twin-screw extruder at a temperature range of 240 to 270
°C, and then was extruded to obtain pellets. Thereafter, the obtained pellets were
dried at 120 °C for 4 hours or more and injected using an 80-ton injection machine
at the same temperature range and at a mold temperature of 100 to 120 °C to prepare
a specimen for measuring physical properties. The physical properties of the prepared
polyester-based resin composition specimen were measured using the following methods,
and the results are shown in Table 2.
* Fluidity (flow index)
[0107] Fluidity was measured at 250 °C under a load of 2.16 kg according to ASTM D1238.
* Tensile strength and elongation
[0108] For a specimen having a thickness of 1/8 inch, the tensile strength and elongation
thereof were measured at a tension speed of 5 mm/minutes according to ASTM D638.
* Flexural strength and flexural modulus
[0109] For a specimen having a thickness of 1/4 inch, the flexural strength and flexural
modulus thereof were measured under conditions of a span of 100 mm and a tension speed
of 5 mm/min according to ASTM D790.
* Viscosity measurement and calculation of viscosity change rate
[0110] FIG. 3 shows a Discovery Hybrid Rheometer (DHR) for measuring the viscosity of a
polyester-based resin composition according to one embodiment of the present invention.
Specifically, FIG. 3A shows an image of a DHR, and FIG. 3B is a drawing for explaining
a method of measuring the viscosity of specimen using the DHR. Using the Discovery
Hybrid Rheometer (DHR) shown in FIG. 3, the viscosity of the polyester-based resin
compositions prepared in Examples and Comparative Examples was measured. At this time,
as measurement conditions, a strain of 0.1 % and a frequency of 1 Hz were set, and
the viscosity of the polyester-based resin compositions was measured at 250 °C and
270 °C, respectively. In addition, viscosity change rate was calculated according
to Equation 1 below.

* Fluidity evaluation (spiral flow length measurement)
[0111] FIG. 4 is an image of a specimen when the spiral flow length of a polyester-based
resin composition according to one embodiment of the present invention is measured.
When measuring spiral flow length, a 120-ton injection machine was used, and injection
pressure was set to 60 bar, cylinder temperature was set to 250 °C, and mold temperature
was set to 50 °C. After the 15th shot, the length (cm) of a polyester-based resin
composition injected from a spiral mold as shown in FIG. 2 was measured. Spiral flow
lengths were measured in the same manner as above at injection pressures of 90 bar
and 120 bar, respectively. In addition, the maximum injection pressure of the polyester-based
resin composition was measured.
* Heat resistance migration (whitening)
[0112] A specimen having a size of 10 mm (width) × 10 mm (length) × 3 mm (thickness) was
allowed to stand in a gear oven at 130 °C for 20 hours, and then the degree of whitening
of the surface of the specimen was evaluated. At this time, when there is no whitening,
it was marked with "None". When whitening was visually observed, it was marked with
"X". When slight whitening was observed, it was marked with "XX". When obvious whitening
was observed, it was marked with "XXX". The degree of whitening of a specimen was
evaluated at 160 °C and 200 °C in the same manner as above, respectively.
* Mold deposit (gas generation)
[0113] FIG. 1 includes drawings for explaining a method of evaluating the amount of gas
generated when molding a polyester-based resin composition according to one embodiment
of the present invention. Using the mold shown in FIG. 1, a polyester-based resin
composition was injected at 250 °C to prepare an injection-molded article. At this
time, the area of gas collected at a gas collection location was measured. The degree
of gas generation in a polyester-based resin composition was evaluated at 270 °C in
the same manner as above.
* Haze evaluation
[0114] FIG. 5 includes an image and a drawing for explaining a method of evaluating the
haze of a composition according to one embodiment of the present invention. Referring
to FIG. 5, the composition specimens prepared in Examples, Additional Examples, and
Comparative Example were placed in a container, and were heated using an oil bath
and maintained at 130 °C for 5 hours. Thereafter, the haze (%) of a glass plate was
measured using a haze meter.
* Evaluation of occurrence of iridescence
[0115] Specimens having a size of 10 mm × 10 mm × 3 mm were prepared using the compositions
prepared in Examples, Additional Examples, and Comparative Example, and aluminum was
deposited on the specimens using a thermal evaporation deposition machine. Then, the
specimens were allowed to stand in a gear oven at 160 °C for 20 hours. Thereafter,
the surface of each specimen was observed using a microscope to determine whether
iridescence occurred. When iridescence was observed, it was marked with "○". When
no iridescence was observed, it was marked with "X". FIG. 6 includes images of a specimen
in which iridescence occurs.
* Injection stress (N): Evaluation of releasability (ejection force, N)
[0116] For quantitative evaluation of the releasability of each sample, pressure delivered
to a mold during injection was compared. A pressure sensor was attached to an ejection
plate located on a moving side during injection, and pressure (ejection force, N)
applied during injection release was expressed as numerical data. For precise comparison,
releasability was measured at least 20 times and an arithmetic mean value was calculated.
[Table 2]
| Classification |
Examples |
Additional Examples |
Comparative Example |
| 1 |
2 |
3 |
4 |
5 |
1 |
2 |
3 |
4 |
1 |
| Fluidity |
42 |
42 |
42 |
42 |
43 |
41 |
40 |
41 |
40 |
42 |
| Tensile strength(kgf/cm2) |
590 |
590 |
590 |
590 |
600 |
580 |
580 |
580 |
580 |
580 |
| Elongation (%) |
20 |
20 |
20 |
20 |
20 |
10 |
10 |
10 |
10 |
10 |
| Flexural strength(kgf/cm2) |
910 |
910 |
910 |
910 |
910 |
910 |
910 |
910 |
910 |
910 |
| Flexural modulus (kgf/cm2) |
26,100 |
26,100 |
26,100 |
26,100 |
27,000 |
26,100 |
26,100 |
26,100 |
26,100 |
26,100 |
| Whitening |
130 °C |
None |
None |
None |
None |
None |
None |
X |
X |
None |
None |
| 160 °C |
None |
None |
None |
None |
None |
XX |
XXX |
XX |
XXX |
X |
| 200 °C |
None |
None |
None |
X |
X |
XXX |
XXX |
XXX |
XXX |
XX |
| Gas generation (mm2) |
250 °C |
|
|
|
|
|
|
|
|
|
|
| 270 °C |
50 |
55 |
90 |
110 |
120 |
69 |
61 |
85 |
130 |
65 |
| Injection stress (N) |
3,200 |
3,000 |
2,350 |
2,200 |
1,980 |
2,800 |
2,180 |
2,500 |
2,500 |
2,500 |
[0117] FIG. 2 shows the results of a whitening test performed on the specimens of Examples
1 to 3 and Example 5, Additional Examples 2 to 4 according to the present invention,
and Comparative Example 1. Referring to Table 2 and FIG. 2, it can be confirmed that
the polyester-based resin composition according to one embodiment of the present invention
has excellent mechanical properties and thermal stability.
[0118] More specifically, in the case of Examples 1 to 5 according to the present invention,
compared to Comparative Example 1, little whitening was observed in a temperature
range of 130 °C to 160 °C. In particular, when comparing Example 2 and Comparative
Example 1 in which other conditions except for the presence or absence of a polar
group are the same, Example 2 exhibits whitening resistance, tensile strength, and
thermal stability superior to those of Comparative Example 1.
[0119] In addition, when comparing Example 2 and Additional Examples 1 to 4 in which other
conditions except for the dropping point and the crystallization temperature (Tm)
of the polar group-containing lubricant are the same, Example 2 exhibits somewhat
higher injection stress than Additional Examples 1 to 4. In addition, Example 2 exhibits
superior whitening resistance to Additional Examples 1 to 4.
[0120] In addition, it can be seen that Examples 1 and 2 show the most suitable mechanical
properties and fluidity for a headlamp bezel.
Example 6
[0121] Polybutylene terephthalate having an intrinsic viscosity of 1.12 dl/g, pentaerythritol
tetrastearate as the ester group-containing lubricant, a phenolic antioxidant as the
antioxidant, and a phenyl group-containing polycarbodiimide as the hydrolysis stabilizer
were mixed to prepare a polyester-based resin composition.
[0122] In this case, based on 100 parts by weight of the polyester-based resin composition,
the content of polybutylene terephthalate was 99.0 parts by weight, the content of
the ester group-containing lubricant was 0.3 parts by weight, the content of the antioxidant
was 0.2 parts by weight, and the content of the hydrolysis stabilizer was 0.5 parts
by weight.
Example 7
[0123] A polyester-based resin composition was prepared in the same manner as in Example
6, except that polybutylene terephthalate having an intrinsic viscosity of 0.91 dl/g
was used instead of the polybutylene terephthalate having an intrinsic viscosity of
1.12 dl/g and the contents of each of the polybutylene terephthalate, the ester group-containing
lubricant, the antioxidant, and the hydrolysis stabilizer were adjusted as shown in
Table 3 below.
Example 8
[0124] A polyester-based resin composition was prepared in the same manner as in Example
6, except that polybutylene terephthalate having an intrinsic viscosity of 1.00 dl/g
was used instead of the polybutylene terephthalate having an intrinsic viscosity of
1.12 dl/g and the contents of each of the polybutylene terephthalate, the ester group-containing
lubricant, the antioxidant, and the hydrolysis stabilizer were adjusted as shown in
Table 3 below.
Additional Example 5
[0125] A polyester-based resin composition was prepared in the same manner as in Example
6, except that polybutylene terephthalate having an intrinsic viscosity of 0.83 dl/g
was used instead of the polybutylene terephthalate having an intrinsic viscosity of
1.12 dl/g and the contents of each of the polybutylene terephthalate, the ester group-containing
lubricant, the antioxidant, and the hydrolysis stabilizer were adjusted as shown in
Table 3 below.
Additional Example 6
[0126] A polyester-based resin composition was prepared in the same manner as in Example
6, except that a mixture of polybutylene terephthalate having an intrinsic viscosity
of 1.00 dl/g and polybutylene terephthalate having an intrinsic viscosity of 0.83
dl/g was used instead of the polybutylene terephthalate having an intrinsic viscosity
of 1.12 dl/g and the contents of each of the polybutylene terephthalate, the ester
group-containing lubricant, the antioxidant, and the hydrolysis stabilizer were adjusted
as shown in Table 3 below.
Additional Example 7
[0127] A polyester-based resin composition was prepared in the same manner as in Example
6, except that a mixture of polybutylene terephthalate having an intrinsic viscosity
of 1.00 dl/g and polybutylene terephthalate having an intrinsic viscosity of 0.83
dl/g was used instead of the polybutylene terephthalate having an intrinsic viscosity
of 1.12 dl/g and the contents of each of the polybutylene terephthalate, the ester
group-containing lubricant, the antioxidant, and the hydrolysis stabilizer were adjusted
as shown in Table 3 below.
Additional Example 8
[0128] A polyester-based resin composition was prepared in the same manner as in Example
6, except that a mixture of polybutylene terephthalate having an intrinsic viscosity
of 1.00 dl/g and polybutylene terephthalate having an intrinsic viscosity of 0.83
dl/g was used instead of the polybutylene terephthalate having an intrinsic viscosity
of 1.12 dl/g and the contents of each of the polybutylene terephthalate, the ester
group-containing lubricant, the antioxidant, and the hydrolysis stabilizer were adjusted
as shown in Table 3 below.
[Table 3]
| Parts by weight |
Examples |
Additional Examples |
| 6 |
7 |
8 |
5 |
6 |
7 |
8 |
| A1 |
99.0 |
|
|
|
|
|
|
| A2 |
|
|
99.0 |
|
40.0 |
59.0 |
79.0 |
| A3 |
|
99.0 |
|
|
|
|
|
| A4 |
|
|
|
99.0 |
59.0 |
40.0 |
20.0 |
| B |
0.3 |
0.3 |
0.3 |
0.3 |
0.3 |
0.3 |
0.3 |
| C |
0.2 |
0.2 |
0.2 |
0.2 |
0.2 |
0.2 |
0.2 |
| D |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
0.5 |
[0129] In Table 3, "A1" represents polybutylene terephthalate having an intrinsic viscosity
of 1.12 dl/g, "A2" represents polybutylene terephthalate having an intrinsic viscosity
of 1.00 dl/g, "A3" represents polybutylene terephthalate having an intrinsic viscosity
of 0.91 dl/g, "A4" represents polybutylene terephthalate having an intrinsic viscosity
of 0.83 dl/g, "B" represents pentaerythritol tetrastearate as the lubricant, "C" represents
the phenolic antioxidant, and "D" represents the phenyl group-containing polycarbodiimide.
In addition, in Table 3, the content of each component is given in parts by weight
based on 100 parts by weight of the polyester-based resin composition.
[0130] The polyester-based resin compositions of Examples 6 to 8 and Additional Examples
5 to 8, which were formulated according to the components and contents shown in Table
3, were used to prepare specimens for measuring physical properties according to the
above-described methods, and the physical properties of the specimens were measured
according to the above-described methods for measuring physical properties. The results
are shown in Table 4 below.
[Table 4]
| Classification |
Examples |
Additional Examples |
| 6 |
7 |
8 |
5 |
6 |
7 |
8 |
| Fluidity |
13 |
43 |
32 |
75 |
55 |
43 |
38 |
| Tensile strength (kgf/cm2) |
590 |
580 |
580 |
580 |
580 |
580 |
580 |
| Elongation(%) |
10 |
10 |
10 |
10 |
10 |
10 |
10 |
| Flexural strength (kgf/cm2) |
920 |
910 |
910 |
910 |
910 |
910 |
910 |
| Flexural modulus (kgf/cm2) |
27,000 |
26,100 |
27,000 |
26,800 |
26,100 |
26,100 |
27,100 |
| Viscosity |
@250 °C |
520 |
240 |
398 |
186 |
161 |
202 |
212 |
| @270 °C |
410 |
112 |
280 |
61 |
40 |
61 |
72 |
| Viscosity change rate(%) |
55 |
64 |
62.5 |
59 |
60.5 |
70.5 |
70 |
| Fluidity evaluation |
@60bar (cm) |
18.2 |
24.5 |
25.0 |
29.8 |
24.6 |
25.5 |
25.0 |
| @90bar (cm) |
24.4 |
32.3 |
31.2 |
39.0 |
32.7 |
33.5 |
32.5 |
| @120bar (cm) |
31.2 |
38.8 |
36.5 |
47.3 |
38.3 |
38.5 |
38.0 |
| Maximum injection pressure (kgf/cm2) |
1,300 |
1,050 |
1,100 |
925 |
985 |
1,060 |
1,130 |
| Gas generation (mm2) |
250 °C |
48 |
52 |
52 |
61 |
55 |
53 |
55 |
| 270 °C |
57 |
62 |
64 |
83 |
74 |
69 |
66 |
[0131] Referring to Table 4, it can be confirmed that the polyester-based resin composition
according to one embodiment of the present invention has excellent mechanical properties
and injection stability. More specifically, compared to Additional Examples 5 to 8
in which a polybutylene terephthalate resin having an intrinsic viscosity of less
than 0.90 dl/g is included, in the case of Examples 6 to 8 in which a polybutylene
terephthalate resin having an intrinsic viscosity of 0.90 to 1.15 dl/g is included,
fluidity, mechanical properties, and injection stability are excellent, and the amount
of gas generated during injection molding is reduced.
Example 9
[0132] 52.5 parts by weight of a first polybutylene terephthalate resin having a relative
viscosity of 1.0 according to ASTM D1243, 40.0 parts by weight of a second polybutylene
terephthalate resin having a relative viscosity of 0.8 according to ASTM D1243, 5.0
parts by weight of a styrene-acrylonitrile copolymer containing 28 % by weight of
acrylonitrile, 0.5 parts by weight of a pentaerythritol-based lubricant, 0.2 parts
by weight of a phenolic antioxidant (hindered phenolic primary antioxidant), and 0.5
parts by weight of an aromatic polycarbodiimide as the hydrolysis stabilizer were
mixed to prepare a composition for automotive headlamp bezels.
Example 10
[0133] A composition for automotive headlamp bezels was prepared in the same manner as in
Example 9, except that a styrene-acrylonitrile copolymer containing 29 % by weight
of acrylonitrile was used.
Example 11
[0134] A composition for automotive headlamp bezels was prepared in the same manner as in
Example 9, except that 3.0 parts by weight of a styrene-acrylonitrile copolymer containing
29 % by weight of acrylonitrile (prepared by two dehydration processes) was used.
Example 12
[0135] A composition for automotive headlamp bezels was prepared in the same manner as in
Example 9, except that 1.0 part by weight of a styrene-acrylonitrile copolymer containing
29 % by weight of acrylonitrile was used.
Additional Example 9
[0136] A composition for automotive headlamp bezels was prepared in the same manner as in
Example 9, except that a styrene-acrylonitrile copolymer containing 24 % by weight
of acrylonitrile was used.
Additional Example 10
[0137] A composition for automotive headlamp bezels was prepared in the same manner as in
Example 9, except that a styrene-acrylonitrile copolymer containing 32 % by weight
of acrylonitrile was used.
Additional Example 11
[0138] 57.5 parts by weight of a first polybutylene terephthalate resin having a relative
viscosity of 1.0 according to ASTM D1243, 40.0 parts by weight of a second polybutylene
terephthalate resin having a relative viscosity of 0.8 according to ASTM D1243, 0.5
parts by weight of a pentaerythritol-based lubricant, 0.2 parts by weight of a phenolic
antioxidant (hindered phenolic primary antioxidant), and 0.5 parts by weight of an
aromatic polycarbodiimide as the hydrolysis stabilizer were mixed to prepare a composition
for automotive headlamp bezels.
[0139] The components and contents included in the compositions of Examples 9 to 12 and
Additional Examples 9 to 11 are shown in Table 5 below.
[Table 5]
| Parts by weight |
Examples |
Additional Examples |
| 9 |
10 |
11 |
12 |
9 |
10 |
11 |
| A1 |
52.5 |
52.5 |
54.5 |
56.5 |
52.5 |
52.5 |
57.5 |
| A2 |
40.0 |
40.0 |
40.0 |
40.0 |
40.0 |
40.0 |
40.0 |
| B1 |
|
|
|
|
5.0 |
|
|
| B2 |
5.0 |
|
|
|
|
|
|
| B3 |
|
5.0 |
3.0 |
1.0 |
|
|
|
| B4 |
|
|
|
|
|
5.0 |
|
| C |
0.9 |
0.9 |
0.9 |
0.9 |
0.9 |
0.9 |
0.9 |
| D |
0.6 |
0.6 |
0.6 |
0.6 |
0.6 |
0.6 |
0.6 |
| E |
1.0 |
1.0 |
1.0 |
1.0 |
1.0 |
1.0 |
1.0 |
[0140] In Table 5, "A1" represents a first polybutylene terephthalate resin having a relative
viscosity of 1.0 according to ASTM D1243, "A2" represents a second polybutylene terephthalate
resin having a relative viscosity of 0.8 according to ASTM D1243, "B1" represents
a styrene-acrylonitrile copolymer containing 24 % by weight of acrylonitrile, "B2"
represents a styrene-acrylonitrile copolymer containing 28 % by weight of acrylonitrile,
"B3" represents a styrene-acrylonitrile copolymer containing 29 % by weight of acrylonitrile,
"B4" represents a styrene-acrylonitrile copolymer containing 32 % by weight of acrylonitrile,
"C" represents a pentaerythritol-based lubricant, "D" represents a phenolic antioxidant,
and "E" represents an aromatic polycarbodiimide as the hydrolysis stabilizer.
[0141] Each of the polyester-based resin compositions of Examples 9 to 12 and Additional
Examples 9 to 11 formulated according to the components and contents shown in Table
5 was used to prepare a specimen for measuring physical properties using the above-described
methods. The physical properties of the specimen were measured using the above-described
methods, and the results are shown in Table 6 below.
Table 6]
| Classification |
Examples |
Additional Examples |
| 9 |
10 |
11 |
12 |
9 |
10 |
11 |
| Fluidity |
40 |
40 |
40 |
40 |
42 |
40 |
41 |
| Tensile strength(kgf/cm2) |
550 |
550 |
550 |
550 |
550 |
550 |
550 |
| Elongation(%) |
10 |
10 |
10 |
10 |
10 |
10 |
10 |
| Flexural strength (kgf/cm2) |
910 |
920 |
910 |
910 |
910 |
910 |
890 |
| Flexural modulus (kgf/cm2) |
27100 |
27100 |
27000 |
27000 |
25200 |
27000 |
26500 |
| Viscosity |
@250 °C |
277 |
191 |
254 |
234 |
250 |
258 |
169 |
| @270 °C |
161 |
151 |
134 |
144 |
153 |
173 |
123 |
| Viscosity change rate(%) |
58 |
20 |
60 |
45 |
48.5 |
42.5 |
23 |
| Fluidity evaluation |
@60bar (cm) |
24.6 |
24.5 |
25.0 |
24.0 |
29.8 |
25.5 |
25.0 |
| @90bar (cm) |
32.7 |
32.3 |
32.5 |
30.5 |
39.0 |
33.5 |
31.2 |
| @120bar (cm) |
38.3 |
38.8 |
38.0 |
37.0 |
47.3 |
38.5 |
36.5 |
| Maximum injection pressure (kgf/cm2) |
985 |
1050 |
1130 |
1110 |
925 |
1060 |
1100 |
| Haze evaluation |
4.8 |
4.3 |
4.1 |
3.3 |
23.0 |
15.0 |
2.1 |
| Gas generation (mm2) |
250 °C |
72 |
58 |
56 |
54 |
80 |
63 |
52 |
| Occurrence of iridescence |
X |
X |
X |
X |
X |
X |
○ |
[0142] Referring to Table 6, it can be confirmed that the composition for automotive headlamp
bezels according to one embodiment of the present invention has excellent fluidity,
mechanical properties, and injection stability, has a low haze value, and rarely exhibits
iridescence, and thus may be suitably used in manufacture of an automotive headlamp
bezel. More specifically, the compositions prepared according to Examples 9 to 12
have excellent fluidity, mechanical properties, and injection stability, have a haze
value of less than 10, and do not exhibit iridescence, and thus may be suitably used
in manufacture of an automotive headlamp bezel. In particular, in the case of Examples
10 to 12, since gas generation is reduced, contamination of a mold due to gas may
be reduced. Thus, a mold cleaning cycle may be increased, thereby improving economic
efficiency.
[0143] In addition, Examples 9 and 10 in which 5.0 % by weight of a styrene-acrylonitrile
copolymer containing 25 to 29 % by weight of acrylonitrile is included have a lower
haze value than Additional Example 9 in which 5.0 % by weight of a styrene-acrylonitrile
copolymer containing acrylonitrile in an amount less than the above range is included
and Additional Example 10 in which 5.0 % by weight of a styrene-acrylonitrile copolymer
containing acrylonitrile in an amount exceeding the above range is included. Based
on these results, it can be seen that Examples 1 and 2 are suitable for application
to automotive headlamp bezels.
[0144] In addition, Additional Example 11 in which a styrene-acrylonitrile copolymer is
not included exhibits the lowest haze value, but exhibits iridescence. Accordingly,
it can be seen that Additional Example 11 is less suitable for application to automotive
headlamp bezels compared to other Examples.